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HS Code |
368557 |
| Product Name | Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate |
| Cas Number | 80887-72-1 |
| Molecular Formula | C8H11F6O5P |
| Molecular Weight | 338.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically >98% |
| Density | 1.492 g/mL at 25°C |
| Solubility | Soluble in common organic solvents (e.g., dichloromethane, chloroform) |
| Storage Conditions | Store at 2-8°C, keep tightly closed |
| Smiles | COC(=O)CP(=O)(OCC(F)(F)F)OCC(F)(F)F |
| Inchi | InChI=1S/C8H11F6O5P/c1-19-7(17)6-21(18,20-2-8(9,10)11)22-3-8(12,13)14/h2-6H2,1H3 |
As an accredited Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mg supplied in a clear, sealed glass vial, labeled with chemical name, quantity, lot number, hazard symbols, and handling instructions. |
| Shipping | **Shipping Description:** Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate should be shipped in a tightly sealed container, protected from moisture and extreme temperatures. Handle as a chemical reagent, ensuring compliance with any applicable regulatory requirements for fluorinated organophosphorus compounds. Appropriate labeling and documentation are required. Choose compatible packaging materials for safe transit. |
| Storage | **Storage Description:** Store Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)phosphonate in a tightly sealed container, protected from moisture and direct sunlight. Keep in a cool, dry, and well-ventilated area away from heat sources, strong acids, bases, and oxidizing agents. Label containers clearly and avoid prolonged exposure to air. Follow all safety and regulatory guidelines for chemical storage and handling. |
Applications of Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate in Industrial ManufacturingBis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate is primarily used by specialty chemical producers in the synthesis of advanced functional materials. The compound serves as a key intermediate for manufacturers operating in high-value chemical sectors, where consistent quality and precise formulation control are critical. Our production adheres to strict internal QC protocols, supporting reliable supply for downstream high-performance applications. 1. Synthesis of Flame Retardant Additives for Engineering PlasticsManufacturers in the engineering plastics sector use this compound to introduce phosphorus and fluorine groups, improving flame resistance for thermoplastic resins. Our material is engaged during the formulation of phosphonate flame retardants, ultimately incorporated by compounding or polymerization with polycarbonate, ABS, or polyamide systems. The synthesis step requires accurate dosing and monitoring to comply with global flame retardant norms. Industry compliance standards
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2. Precursor for Agrochemical Active IngredientsCrop protection manufacturers select this phosphonate ester as a building block for synthesizing novel organophosphorus pesticides, especially for products requiring strong metabolic stability. The compound participates in selective phosphorylation steps during the design of herbicide and insecticide actives, supporting robust structure-activity relationships and regulatory traceability. Industry compliance standards
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3. Pharmaceutical Intermediate for Antiviral AgentsThe pharmaceutical sector uses this compound in the synthesis of phosphate prodrugs for antiviral therapies, benefitting from the compound’s fluorinated structure to impart bioavailability. Medicinal chemistry operations utilize precise feeds of the material in their flow synthesis or batch process to generate high-purity prodrug phosphonates compatible with cGMP frameworks for eventual tableting. Industry compliance standards
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4. Intermediate in Specialty Coating Raw MaterialsSpecialty coating manufacturers use this compound to create phosphonate-functional acrylics and polyurethanes, aiming for chemical resistance on industrial substrates. It undergoes reaction during resin synthesis, providing sites for increased adhesion and solvent resistance, and supports production of high-durability coatings compliant with modern safety and emission controls. Industry compliance standards
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5. Precursor in Synthesis of High-Performance Lubricant AdditivesThis compound functions as a precursor during the production of phosphorus-containing lubricant additives. Process engineers use it in additive synthesis to introduce anti-wear and friction modifier properties. It is essential in manufacturing advanced lubricants for machinery exposed to extreme pressures and temperatures, where traceability of raw material input impacts final additive certification. Industry compliance standards
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From the earliest formulations in our plant, Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate positioned itself as both an achievement in process engineering and a direct answer to a critical set of demands from synthetic chemists. Building the process for this compound required more than routine handling. Highly fluorinated raw materials require specific material linings in our reactors and transfer lines to prevent both trace contamination and equipment corrosion, which directly shapes purity and batch consistency. Our experience running this material at scale taught an important lesson: controlling air and moisture during both charging and post-reaction workup determines the stability of the final phosphonate much more than with typical alkyl or aryl analogues.
Within the product portfolio at our factory, phosphonate esters take up an outsized role in research and manufacturing conversations. Yet not every variant draws the repeated requests for scale-up as much as this one. Industrial partners and academic groups looking for strong carbon-phosphorus bonds with built-in fluorinated groups come to us frequently, and most seek the reproducibility of downstream reaction profiles they achieve with our material. Consistency in melting point, color, and even subtle volatility signals allows them to shorten purification steps for subsequent coupling reactions. For scale chemists, downtime from poorly behaving intermediates translates straight to unwanted cost and waste.
Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate distinguishes itself from other organophosphonate options through the unique properties imparted by its trifluoroethyl substituents. In synthesis campaigns, the electron-withdrawing nature of this group tunes reactivity at the phosphorus center in ways typical ethyl or methyl groups cannot match. That tuning extends to thermal and hydrolytic stabilities; compounds that rely on labile phosphonates for their activity benefit from the backbone strength the trifluoroethyl chains deliver. Our production batches always display a distinctive sharpness in NMR spectra—again, a function of the fluorine atoms—allowing process chemists to monitor conversion with much greater precision during alkylations or methoxy insertions.
Manufacturing equipment longevity is another practical dimension. The presence of fluorinated chains acts almost like a built-in resistance factor against unwanted side reactions with steel, glass, or PTFE-lined vessels. We have witnessed firsthand the reduction in trace peroxide formation and less fouling buildup across the heat exchangers during long production runs compared to phosphonates featuring only hydrocarbon substituents. This prolongs campaign life and lowers the frequency of system flushes, both of which directly matter to efficiency on the plant floor.
Every run aiming to deliver Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate requires stringent monitoring of temperature and pressure. The handling of the trifluoroethyl intermediates, due to their volatility and reactivity, shaped our decision to install closed handling and dedicated in-line sensors. Years of analyzing contaminants taught us to limit not only water but also adventitious acid residues. Even a few parts-per-million elevates the degradation rate of this phosphonate under storage conditions and during transport. For packed columns and crystallizers, we adopted a protocol to clean with non-polar solvents first, a direct learning from slow residue buildups that caused yield drifts in earlier years.
We learned to keep production independent from runs involving sulfur, phosphorus pentachloride, or halogenated aromatics within the same cycle. Cross-contamination had too much of an impact not just on analytical numbers, but on customer synthesis outcomes down the line. This type of control meant more up-front operational burden, but the result was clear: we now hear of fewer downstream conversion failures or difficult purifications than in the days before these protocols. Our plant chemists cite decreased lot-to-lot variability in both GC and HPLC traces, a central metric for anyone designing multi-kilo syntheses using this phosphonate as a key step.
Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate sees most of its daily movement into the hands of synthetic chemists designing advanced intermediates for pharmaceuticals and agrochemicals. Its trifluoromethyl groups bring value where solubility control and metabolic stability matter in active agents. In early phase discovery, this molecule’s clean reaction profile means fewer purification headaches and, based on feedback over years, lower failure rates at scale-up.
Polymer research teams routinely request samples for their new fluorinated materials. The ability to anchor a phosphonate backbone and further decorate the system through controlled substitutions on the methoxycarbonylmethyl group makes this phosphonate a building block. Researchers working on specialty fluorinated surfactants and flame retardants provide us with testimonials about how the presence of trifluoroethyl enhances both fire resistance and material integrity at elevated temperatures, relative to non-fluorinated analogs. Occasionally, experts from electronics projects contact us, drawn by the insulating properties and high breakdown voltages that fluorinated organophosphonates bring to specialty coatings and dielectric layers.
Each conversation with technical partners circles back to what sets this material apart from stock dialkyl phosphonates. The fluorinated side chains resist metabolic and hydrolytic breakdown in a way the simple ethyl or methyl esters do not. Medicinal chemists working on lead candidate optimization emphasize the clear difference in half-lives for their test compounds, which lets them push candidate molecules further before reformulation becomes necessary. Environmental stability means less risk of unexpected transformation under light, heat, or during shipping.
Colleagues in the agricultural space report improved shelf-life for certain bioactive agents developed with this phosphonate scaffold. Their in-house test plots show less leaching and slower breakdown compared to older products. That feedback loop directly influences how we adjust both upstream QA checkpoints and downstream packing: packaging used for non-fluorinated products rarely meets the vapor containment standards this material warrants, and adjusting to this has improved both customer satisfaction and reduced internal product loss.
Years of producing this compound in-house changed our approach to everything from procurement to batch records. We engage with suppliers of trifluoroethanol and methoxyacetate, for instance, to guard against subtle impurity trends that only show up in long-term storage tests. Our QA team runs parallel aged-sample programs, ensuring we spot degradation channels before shipments leave the gate. These measures may not sound headline-worthy, but they minimize field complaints and increase the likelihood that new users become repeat buyers.
Inside our lab suites, the process chemists run simulation batches with the same glassware and protocols we recommend to heavy users. These trial runs proved critical after receiving reports a few years ago about small but reproducible impurity formation during specific Grignard couplings involving the phosphonate. Working these issues backwards, we reformulated a key purification step—removing a trace peroxide-catalyzed byproduct—so that downstream chemistry would remain predictable. The most successful outcomes, from our own process improvements, come when we listen carefully to where our customers say things go wrong, and then redesign the route to prevent a repeat event.
In practice, nothing beats the confidence that comes from pulling a fresh sample, running an NMR or LC/MS, and seeing that the batch aligns with historical samples across all key peaks and retention times. Our strongest relationships with end users grew from cases where last-minute changes or unexpected needs pushed us to double down on batch monitoring, careful stabilization during packing, or even revisiting the drying process to reduce residual solvents by an order of magnitude.
We sometimes receive questions about switching from a methyl or ethyl phosphonate to the trifluoroethyl version in pilot plant settings. After hundreds of runs, our experience shows that the transition rarely demands more than modest equipment and process tweaks. The main adjustment often centers on vapor control and solvent choice, with acetonitrile or chlorinated solvents usually delivering better results for the more volatile, fluorinated compounds. These details show up only after observing cycle-after-cycle outcomes, and point to the silent value of direct hands-on manufacturing experience.
The market for specialty fluorinated organophosphonates evolved quickly since our first lot hit the shelves. Consistency in both supply and performance plays a big role. We invest in raw material validation, not just for purity, but to ensure consistent physical properties like viscosity and refractive index across shipments. This extra layer of control means downstream users spend less time troubleshooting and more time advancing their own work.
In our production logs, the best batches always track back to an extra attention to minor variables; even the temperature of addition for the methoxyacetate or the order of base charging leaves a fingerprint on impurity profile and long-term compound stability. These are not abstract details. They drive outcomes in kilo-scale runs at customer sites, and occasionally in regulatory approvals where trace byproducts—or their absence—make a difference in downstream filings.
Working hands-on with Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate means contending with more than chemical hazards. Our facility adjusted its air handling and spill prevention systems to match the low-vapor pressure and high volatility associated with fluorinated intermediates. Years ago, we shifted to a double-contained transfer system for both charging and discharge steps. This change cut fugitive emissions by over half and reduced operator exposures, protecting both our team and nearby communities.
Waste management strategies developed in our plant benefit from the compound's resistance to rapid breakdown. Instead of standard caustic neutralization, which fails to fully decompose the fluorinated backbone, we partner with specialty incineration facilities. The increased cost is justified by the peace of mind knowing persistent organofluorine residues are not entering waste streams. This kind of strategic partnership took time to establish but now stands as one of the stronger environmental protections in our manufacturing value chain.
The journey of Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate from reactor to package finish centers around ensuring reliable outcomes for users. From day one, our technical sales and support teams document which reaction types cause end-users trouble, sometimes running model reactions in house to refine expected behaviors. Our plant team holds quarterly reviews with frequent buyers where we openly discuss variance trends and brainstorm process modifications. In a few cases, we even co-run test batches with academic collaborators pushing the boundaries of fluorinated chemistry.
This way of doing business—one that values feedback cycles and real-world evidence over simple spec compliance—helped us refine storage protocols and optimize the grade of product offered. Such two-way discussions led to improvements such as custom packaging options and guidance on ideal storage temperatures for minimizing long-term decomposition.
Looking across our spectrum of organophosphonates, Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate stands apart in practical performance. While generic dialkyl or aryl analogues offer lower cost and easy access, the ability of the trifluoroethyl-substituted version to withstand aggressive conditions, both in the plant and under real-world applied settings, remains unmatched. We see the difference frequently. Synthesis yields stay robust across a greater range of conditions, impurity levels trend lower, and shelf-life remains stable even as storage conditions fluctuate.
The formula’s design, balancing an electron-withdrawing fluorinated group with a reactive methoxycarbonylmethyl, gives users flexibility unavailable in classic phosphonates. Downstream transformations proceed with cleaner profiles, letting process chemists sidestep purification bottlenecks that slow timelines and inflate costs. Those developing new active compounds for regulated fields—where small differences in structure and impurity profile can mean the difference between approval and rejection—tend to find their expectations met more reliably with this compound compared to less robust options.
Some manufacturers attempt to offer shortcuts or lower costs by blending or partially substituting reagents, but our long-term records show such decisions translate to variable product and more QA failures. Every time we stuck closely to full-traceability sourcing, especially with the more demanding trifluoroethyl raw materials, both our yields and customer experiences improved. Investment in raw material tracking—right down to secondary containment and in-house analytical verification—has paid off many times over through fewer product holds and field complaints.
We advocate for close communication between manufacturer and end user, never taking specs for granted but confirming success stories and pain points over many cycles of use. Our quality assurance team welcomes records, samples, and even analytical traces from the field, bringing them into regular process improvement meetings for direct impact. Such partnerships rarely make for splashy marketing but result in deep, cumulative improvements that build supplier trust.
Scientific trends in fluorinated phosphonate use only intensify, especially as regulatory and performance standards increase year-to-year. Our commitment is not just to produce a stable supply of high-purity material, but to adjust and advance our own protocols in line with emerging needs. Frequent internal audits, supplier assessments, and feedback loops with downstream teams drive us to both innovate and minimize variability. In our own facility, every process or packaging innovation comes from tackling feedback and observed issues at the very root, never from accepting the status quo.
Every cycle working with Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate strengthens our conviction that hands-on, detail-oriented manufacturing—supported by a feedback-rich environment—brings the industry closer to reliable application breakthroughs. The lessons we learn from repeated direct experience carry forward, shaping each batch and, in turn, each new innovation built from our product.
The shift toward more specialized, high-performance building blocks in chemical synthesis and materials science shows no sign of stopping. As a chemical manufacturer, we view Bis(2,2,2-Trifluoroethyl) (Methoxycarbonylmethyl)Phosphonate not just as another SKU, but as a marker of how industry standards and real-world needs co-evolve. Each advancement—in synthesis, formulation, management of byproducts, or packaging—stems directly from our ongoing conversation with science and technology users worldwide. The value lies in the precision, stability, and reliability we can transfer outwards from our process into yours.